| ID: 132088597 | Neanderthal introgressed variant-containing enhancer experimental_1250 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169531606..169531775) | | |
| ID: 129931895 | ATAC-STARR-seq lymphoblastoid active region 2075 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169604869..169604978) | | |
| ID: 129931894 | ATAC-STARR-seq lymphoblastoid silent region 1546 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169485589..169485768) | | |
| ID: 129931893 | ATAC-STARR-seq lymphoblastoid active region 2072 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169485349..169485408) | | |
| ID: 129931892 | ATAC-STARR-seq lymphoblastoid active region 2070 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169161785..169162044) | | |
| ID: 129388627 | MPRA-validated peak449 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169539087..169539287) | | |
| ID: 129388626 | MPRA-validated peak448 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169526607..169526807) | | |
| ID: 129388625 | MPRA-validated peak447 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169510738..169510938) | | |
| ID: 127270800 | H3K4me1 hESC enhancer GRCh37_chr1:169555695-169556194 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169586457..169586956) | | |
| ID: 127270799 | H3K4me1 hESC enhancer GRCh37_chr1:169555193-169555694 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169585955..169586456) | | |
| ID: 127270798 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:169226550-169227154 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169257312..169257916) | | |
| ID: 127270797 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:169225944-169226549 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169256706..169257311) | | |
| ID: 127270796 | NANOG hESC enhancer GRCh37_chr1:169185155-169185723 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169215917..169216485) | | |
| ID: 126805912 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:169336872-169338071 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169367634..169368833) | | |
| ID: 120893165 | Sharpr-MPRA regulatory region 5964 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169485951..169487001) | | |
| ID: 112577512 | Sharpr-MPRA regulatory region 2803 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169576331..169576625) | | |
| ID: 57821 | coiled-coil domain containing 181 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169394870..169460669, complement) | C1orf114 | 620891 |
| ID: 29922 | NME/NM23 family member 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169132531..169367797, complement) | CFAP67, MN23H7, NDK 7, NDK7, nm23-H7 | 613465 |
| ID: 10560 | solute carrier family 19 member 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169463909..169485970, complement) | TC1, THMD1, THT1, THTR1, TRMA | 603941 |
| ID: 8548 | basic leucine zipper nuclear factor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169368195..169396575) | GOLGIN-45, JEM-1, JEM-1s, JEM1 | 608692 |